newborn hearing screening - world health organization€¦ · for newborns identified with hearing...

3
Bahrain Medical Bulletin, Vol. 38, No. 3, September 2016 148 Hearing loss is a well-documented congenital abnormality. It has an impact on the quality of life of the patient, the family members and society 1 . Hearing loss is known to affect both cognitive and speech-language development which eventually lead to impaired communication 1,2 . A congenital hearing loss could be a handicap if not identified early 3 . Newborn hearing screening plays a major role in early detection of hearing loss, especially in those at risk. Such a screening was conceived based on two concepts: the critical period for optimal language skills development and early intervention produces better outcomes; managing hearing impairments have been shown to improve communication 4 . In 2007, the Joint Committee on Infant Hearing (JCIH) recommended universal detection of hearing loss in newborns and infants and stated that all infants with hearing loss should be identified before three months of age and receive intervention by six months. To gain access to most infants, the JCIH endorsed evaluation before hospital discharge 5 . According to a technical report by American Speech-Language-Hearing Association (ASHA) in 2004, hearing loss has a severe impact on children before speech development 6 . By intervention at the earliest age possible, this developmental gap, caused by hearing loss, could Newborn Hearing Screening Sherin Anne George, BSc, MASLP* Arwa Alawadhi, MBBCh BAO** Hiba Al Reefy, AFRCS, FRCS-ORL HNS, CCT*** Andrew Riskalla, FRCS, DOHNS**** Background: Congenital hearing loss has a major impact on both cognitive and speech-language development which eventually leads to impaired communication and a lower socio-economic status. Objective: To evaluate the result of newborn hearing screening. Design: A Retrospective Study. Setting: NICU and Post-Natal Ward, King Hamad University Hospital, Bahrain. Method: A total of 1,834 babies were screened at the time of discharge, using Transient-Evoked Oto-Acoustic Emissions. Infants who failed the screening test were scheduled for a second screening test. Infants who failed the second screening test were tested with Auditory Brainstem Response (ABR). Result: Five infants were identified with hearing impairment out of 1,834 or 272 per 100,000. The incidence was 0.27% in the infants screened from October 2012 to December 2015 in the hospital. Conclusion: Five infants were identified with hearing loss according to JCIH standards and advised early intervention. The study could be used to plan services and strategies in the hospital for newborns identified with hearing loss at a very early age to offset the long term consequences of hearing loss. Bahrain Med Bull 2016; 38 (3): 148 - 150 be bridged. Studies have suggested that earlier interventions had better outcomes 3,7,8 . Newborn hearing screening is universally performed using Oto-Acoustic Emissions (OAE) and Auditory Brainstem Response (ABR). Newborn infants at risk should be tested as soon as possible; those could be having family history of deafness or admitted to neonatal intensive care for more than 5 days or ECMO, had assisted ventilation, exposed to ototoxic medications (gentamycin and tobramycin) or loop diuretics (furosemide/Lasix), and had hyperbilirubinemia which required exchange transfusion; other condition which put infants at risk could be in utero CMV*, herpes, rubella, syphilis and toxoplasmosis, craniofacial anomalies and syndromes, such as neurofibromatosis, osteopetrosis and Usher syndrome, Waardenburg, Alport, Pendred and Jervell and Lange-Nielson, Hunter syndrome, Friedrich’s ataxia, and Charlotte-Marie- Tooth syndrome 5 . Most units utilize the two-phase newborn hearing strategy 9 . The first phase involves the initial screening of the infant using TEOAE followed by the second phase, the retest. If an infant fails the retest screening, the infant is referred for a diagnostic * Audiologist ** Senior House Officer *** Consultant, Head of Department **** Consultant Department of ENT King Hamad University Hospital The Kingdom of Bahrain E-mail: [email protected]

Upload: others

Post on 12-Jun-2020

1 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: Newborn Hearing Screening - World Health Organization€¦ · for newborns identified with hearing loss at a very early age to offset the long term consequences of hearing loss. Bahrain

Bahrain Medical Bulletin, Vol. 38, No. 3, September 2016

148

Hearing loss is a well-documented congenital abnormality. It has an impact on the quality of life of the patient, the family members and society1. Hearing loss is known to affect both cognitive and speech-language development which eventually lead to impaired communication1,2. A congenital hearing loss could be a handicap if not identified early3.

Newborn hearing screening plays a major role in early detection of hearing loss, especially in those at risk. Such a screening was conceived based on two concepts: the critical period for optimal language skills development and early intervention produces better outcomes; managing hearing impairments have been shown to improve communication4. In 2007, the Joint Committee on Infant Hearing (JCIH) recommended universal detection of hearing loss in newborns and infants and stated that all infants with hearing loss should be identified before three months of age and receive intervention by six months. To gain access to most infants, the JCIH endorsed evaluation before hospital discharge5. According to a technical report by American Speech-Language-Hearing Association (ASHA) in 2004, hearing loss has a severe impact on children before speech development6. By intervention at the earliest age possible, this developmental gap, caused by hearing loss, could

Newborn Hearing Screening

Sherin Anne George, BSc, MASLP* Arwa Alawadhi, MBBCh BAO** Hiba Al Reefy, AFRCS, FRCS-ORL HNS, CCT*** Andrew Riskalla, FRCS, DOHNS****

Background: Congenital hearing loss has a major impact on both cognitive and speech-language development which eventually leads to impaired communication and a lower socio-economic status.

Objective: To evaluate the result of newborn hearing screening.

Design: A Retrospective Study.

Setting: NICU and Post-Natal Ward, King Hamad University Hospital, Bahrain.

Method: A total of 1,834 babies were screened at the time of discharge, using Transient-Evoked Oto-Acoustic Emissions. Infants who failed the screening test were scheduled for a second screening test. Infants who failed the second screening test were tested with Auditory Brainstem Response (ABR).

Result: Five infants were identified with hearing impairment out of 1,834 or 272 per 100,000. The incidence was 0.27% in the infants screened from October 2012 to December 2015 in the hospital. Conclusion: Five infants were identified with hearing loss according to JCIH standards and advised early intervention. The study could be used to plan services and strategies in the hospital for newborns identified with hearing loss at a very early age to offset the long term consequences of hearing loss.

Bahrain Med Bull 2016; 38 (3): 148 - 150

be bridged. Studies have suggested that earlier interventions had better outcomes3,7,8.

Newborn hearing screening is universally performed using Oto-Acoustic Emissions (OAE) and Auditory Brainstem Response (ABR). Newborn infants at risk should be tested as soon as possible; those could be having family history of deafness or admitted to neonatal intensive care for more than 5 days or ECMO, had assisted ventilation, exposed to ototoxic medications (gentamycin and tobramycin) or loop diuretics (furosemide/Lasix), and had hyperbilirubinemia which required exchange transfusion; other condition which put infants at risk could be in utero CMV*, herpes, rubella, syphilis and toxoplasmosis, craniofacial anomalies and syndromes, such as neurofibromatosis, osteopetrosis and Usher syndrome, Waardenburg, Alport, Pendred and Jervell and Lange-Nielson, Hunter syndrome, Friedrich’s ataxia, and Charlotte-Marie-Tooth syndrome5.

Most units utilize the two-phase newborn hearing strategy9. The first phase involves the initial screening of the infant using TEOAE followed by the second phase, the retest. If an infant fails the retest screening, the infant is referred for a diagnostic

* Audiologist** Senior House Officer*** Consultant, Head of Department**** Consultant

Department of ENTKing Hamad University HospitalThe Kingdom of BahrainE-mail: [email protected]

Page 2: Newborn Hearing Screening - World Health Organization€¦ · for newborns identified with hearing loss at a very early age to offset the long term consequences of hearing loss. Bahrain

Bahrain Medical Bulletin, Vol. 38, No. 3, September 2016

149

ABR evaluation. This minimizes a false positive response that is inevitable during screening.

The aim of this study is to evaluate the results of the newborn hearing screening.

METHOD

The newborn hearing screening was performed from October 2012 to December 2015. Newborns were screened at the time of discharge using Transient-Evoked Oto-Acoustic Emissions (TEOAE).

A two-phased hearing screening was implemented. The first phase was performed using TEOAE. The second phase was performed using TEOAE a week after discharge for those who failed the first test. The second phase was performed using TEOAE. Failed test could be due to irritable and uncooperative infants, in which a repeat test is required.

Newborns who failed the second test were tested with Auditory Brainstem Response (ABR) under natural sleep or with the help of mild sedation (chloral hydrate).

Not achieving a normal ABR result (evidence of Wave V at 40dBnHL) is a diagnostic criterion for hearing impairment which mandates counseling and hearing impairment management.

RESULT

A total of 1,834 infants were screened in the first stage. Out of which, 1,687 passed the test and were discharged. One hundred forty-seven (8.01%) of these failed the first screening test; out of which, 138 (7.5%) infants passed the second screening test and 9 (0.49%) failed. The nine infants were recommended for diagnostic ABR. Four (0.21%) infants passed the ABR test revealing normal bilateral hearing and 5 (0.27%) infants failed indicating bilateral severe to profound hearing loss (due to the absence of Wave V at 100dBnHL). The five infants had certain risk factors (one had severe neonatal jaundice, 2 had family history of hearing loss and 2 were preterm babies). Therefore, the incidence of the hearing impairment was 0.27% out of 1834 or 272 per 100000 infants for the period from 2012 to 2015 in the hospital, see figure 1.

Four (n=4, 0.21%) infants were admitted to NICU and one (n=1, 0.05%) was in the pediatric ward (P-value=0.091). However, logistic regression analysis of the influence of admission to NICU did not reveal any significant effect on the incidence of hearing loss (Odds ratio =0.250, 95% CI: 0.013 – 4.729).

DISCUSSION

A study found that TEOAE specificity is 98.8% and sensitivity is 66.7% for neonatal hearing screening10. Failure of the first hearing screening could be due to the presence of ear canal obstruction; therefore, a repeat test is recommended11.

In this study, the incidence is small compared to 2.0% in Kuwait12. A study in Egypt has identified 9 of every 1000 live births to have hearing loss13. On the other hand, a study in Iran reported 1.8 out of every 1000 live births14. Similarly, a study in Oman revealed a rate of 0.12%15. In our study, 2.6 out of every 1000 live births were assumed to have hearing loss, it is similar to the United Kingdom, which is estimated to be one out of every 1000 live births16. A review of literature in the US has revealed 0.22 to 3.61 per 1000 live births17.

Our incidence revealed to be less than that of other studies; it could be due to the small sample size from one tertiary center in Bahrain. The five infants that were identified with sensorineural hearing loss were counseled regarding the best early intervention options, such as cochlear implantation. Further efforts have been made to refer these infants to centers where cochlear implantations are performed.

CONCLUSION

Five infants were identified with hearing loss according to JCIH standards and advised early intervention.

It is vital to increase awareness regarding the importance of early screening and applying it to all newborns in the

! ""

1834 Patients Screened

147 Failed the First Test

1687 Passed the First Test

9 Failed the Second Test

138 Passed the Second Test

9 Tested with ABR

4 Passed ABR Test

5 Failed ABR

Figure 1: Results of Neonatal Screening (N=5)

Figure 2: Children Diagnosed with Hearing Loss Admission (N=5)

Newborn Hearing Screening

Page 3: Newborn Hearing Screening - World Health Organization€¦ · for newborns identified with hearing loss at a very early age to offset the long term consequences of hearing loss. Bahrain

Bahrain Medical Bulletin, Vol. 38, No. 3, September 2016

150

country. Families, healthcare professionals and social workers should be educated and made to understand that all patients deserve an equal chance for a more promising quality of life.

Further multicenter prospective study is recommended to estimate the national incidence.__________________________________________________

Author Contribution: All authors share equal effort contribution towards (1) substantial contribution to conception and design, acquisition, analysis and interpretation of data; (2) drafting the article and revising it critically for important intellectual content; and (3) final approval of manuscript version to be published. Yes.

Potential Conflicts of Interest: None.

Competing Interest: None.

Sponsorship: None.

Submission Date: 14 March 2016.

Acceptance Date: 12 June 2016.

Ethical Approval: Approved by the Research and Ethics Committee, King Hamad University Hospital, Bahrain.

REFERENCES

1. Emmett SD, Francis HW. The Socioeconomic Impact of Hearing Loss in U.S. Adults. Otol Neurotol 2015; 36(3):545-50.

2. Wake M, Hughes E, Poulakis Z, et al. Outcomes of Children with Mild-Profound Congenital Hearing Loss at 7 to 8 Years: A Population Study. Ear Hear 2004; 25(1):1-8.

3. McConkey Robbins A, Koch D, Osberger MJ, et al. Effect of Age at Cochlear Implantation on Auditory Skill Development in Infants and Toddlers. Arch Otolaryngol Head Neck Surg 2004; 130(5):570-4.

4. Lim G, Fortaleza K. Overcoming Challenges in Newborn Hearing Screening. J Perinatol 2000; 20(8 Pt2):S138-42.

5. American Academy of Pediatrics, Joint Committee on Infant Hearing. Year 2007 Position Statement: Principles and Guidelines for Early Hearing Detection and Intervention Programs. Pediatrics 2007 Oct; 120(4):898-921.

6. American Speech-Language-Hearing Association. Technical Report Cochlear Implants. 2004. http://www.asha.org/policy/TR2004-00041.htm. Accessed on 28 October 2015.

7. Sharma A, Dorman MF, Spahr AJ. A Sensitive Period for the Development of the Central Auditory System in Children with Cochlear Implants: Implications for Age of Implantation. Ear Hear 2002; 23(6):532-9.

8. Svirsky MA, Teoh SW, Neuburger H. Development of Language and Speech Perception in Congenitally, Profoundly Deaf Children as a Function of Age at Cochlear Implantation. Audiol Neurootol 2004; 9(4):224-33.

9. Cavalcanti HG, Melo LP, Buarque LF, et al. Overview of Newborn Hearing Screening Programs in Brazilian Maternity Hospitals. Braz J Otorhinolaryngol 2014; 80(4):346-53.

10. Yousefi J, Ajalloueyan M, Amirsalari S, et al. The Specificity and Sensitivity of Transient Otoacoustic Emission in Neonatal Hearing Screening Compared with Diagnostic Test of Auditory Brain Stem Response in Tehran Hospitals. Iran J Pediatr 2013; 23(2):199-204.

11. Eiserman W, Shisler L, Foust T, et al. Screening for Hearing Loss in Early Childhood Programs. Early Childhood Research Quarterly 2007; 22(1):105-117.

12. Al-Kandari JM, Alshuaib WB. Newborn Hearing Screening in Kuwait. Electromyogr Clin Neurophysiol 2007; 47(6):305-13.

13. Kamal N. Newborn Hearing Screening: Opportunities and Challenges. Egyptian Journal of Ear, Nose, Throat and Allied Sciences. 2013; 14.2:55-8.

14. Haghshenas M, Zadeh P, Javadian Y, et al. Auditory Screening in Infants for Early Detection of Permanent Hearing Loss in Northern Iran. Ann Med Health Sci Res 2014; 4(3):340-4.

15. Khandekar R, Khabori M, Jaffer Mohammed A, et al. Neonatal Screening for Hearing Impairment: The Oman Experience. International Journal of Pediatric Int J Pediatr Otorhinolaryngol 2006; 70(4):663-70.

16. Fortnum HM, Summerfield AQ, Marshall DH, et al. Prevalence of Permanent Childhood Hearing Impairment in the United Kingdom and Implications for Universal Neonatal Hearing Screening: Questionnaire Based Ascertainment Study. BMJ. 2001; 323(7312):536-40.

17. Mehra S, Eavey RD, Keamy DG Jr. The Epidemiology of Hearing Impairment in the United States: Newborns, Children, and Adolescents. Otolaryngol Head Neck Surg 2009; 140(4):461-72.

18. Venail F, Vieu A, Artieres F, et al. Educational and Employment Achievements in Prelingually Deaf Children Who Receive Cochlear Implants. Arch Otolaryngol Head Neck Surg 2010; 136(4):366-72.

19. Geers AE, Nicholas JG, Sedey AL. Language Skills of Children with Early Cochlear Implantation. Ear Hear 2003; 24(1 Suppl):46S-58S.

20. Kasen S, Ouellette R, Cohen P. Mainstreaming and Postsecondary Educational and Employment Status of a Rubella Cohort. Am Ann Deaf 1990 Spring; 135(1):22-6.